Singh D, Jarrell H C, Florio E, Fenske D B, Grant C W
Department of Biochemistry, University of Western Ontario, London, Canada.
Biochim Biophys Acta. 1992 Jan 31;1103(2):268-74. doi: 10.1016/0005-2736(92)90096-5.
The role of glycosphingolipid fatty acid alpha-hydroxylation as a modulator of glycolipid organization and dynamics was considered by 2H-NMR in bilayer membranes. For these experiments, galactosylceramides were prepared in which the natural fatty acid mixture was replaced with perdeuterated 18-carbon hydroxylated or non-hydroxylated stearic acid. The L-stereoisomer of N-(alpha-OH-stearoyl-d34)galactosylceramide and its naturally-occurring D-alpha-OH analogue, were isolated for independent study. Bilayers were formed using 10 mol% galactosylceramide in a shorter chain phospholipid, dimyristoylphosphatidylcholine, in an attempt to reproduce several features of glycolipid-phospholipid interactions typical of cell membranes. Spectra of deuterated galactosylceramide in gel phase phospholipid membranes indicated that alpha-hydroxylation led to greater motional freedom and/or conformational disorder, with no measurable difference between D- and L-alpha-OH fatty acid derivatives. In fluid phosphatidylcholine bilayers the effects were modest. Glycolipid fatty acid hydroxylation led to broadening of the range of order parameters associated with methylene groups near the membrane surface (frequently referred to as the 'plateau region') - this effect being more marked for the naturally-occurring (D) stereoisomer. The degree of overall molecular order sensed by the glycolipid fatty acid chain in a fluid host matrix was minimally affected by alpha-hydroxylation; although the plateau region of the D isomer was slightly more ordered than that of the L isomer and the non-hydroxylated species. These results suggest that a significant aspect of the alpha-hydroxy group effect on glycosphingolipid behaviour in bilayer membranes with low glycolipid content was interference with glycolipid packing amongst host phospholipids in the upper portion of the acyl chains. For the D stereoisomer, there was some evidence that the hydroxy group led to strengthening of interlipid interaction near the membrane surface.
通过双层膜中的2H-NMR研究了糖鞘脂脂肪酸α-羟基化作为糖脂组织和动力学调节剂的作用。在这些实验中,制备了半乳糖神经酰胺,其中天然脂肪酸混合物被全氘代的18碳羟基化或非羟基化硬脂酸取代。分离出N-(α-OH-硬脂酰-d34)半乳糖神经酰胺的L-立体异构体及其天然存在的D-α-OH类似物进行独立研究。使用10 mol%的半乳糖神经酰胺与较短链的磷脂二肉豆蔻酰磷脂酰胆碱形成双层膜,试图重现细胞膜中典型的糖脂-磷脂相互作用的几个特征。凝胶相磷脂膜中氘代半乳糖神经酰胺的光谱表明,α-羟基化导致更大的运动自由度和/或构象无序,D-和L-α-OH脂肪酸衍生物之间没有可测量的差异。在流体磷脂酰胆碱双层膜中,这种影响较小。糖脂脂肪酸羟基化导致与膜表面附近亚甲基相关的有序参数范围变宽(通常称为“平台区”)——这种影响在天然存在的(D)立体异构体中更为明显。在流体宿主基质中,糖脂脂肪酸链感知到的整体分子有序程度受α-羟基化的影响最小;尽管D异构体的平台区比L异构体和非羟基化物种的平台区稍微更有序一些。这些结果表明,在糖脂含量低的双层膜中,α-羟基对糖鞘脂行为的显著影响方面是干扰了酰基链上部宿主磷脂之间的糖脂堆积。对于D立体异构体,有一些证据表明羟基导致膜表面附近脂质间相互作用增强。